# FDA Inspection 804091 - nSpire Health Ltd - September 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/nspire-health-ltd/8d925d12-4274-4f3e-bd34-e043b05b3cf0
Source feed: FDA_Inspections

> FDA Inspection 804091 for nSpire Health Ltd on September 20, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 804091
- Company Name: nSpire Health Ltd
- Inspection Date: 2012-09-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 942270 - 2015-08-19](https://www.keypedia.com/records/fda_inspections/nspire-health-ltd/fd73aedd-6ed5-4280-8156-5e932de49a2a)
- [FDA Inspection 804091 - 2012-09-20](https://www.keypedia.com/records/fda_inspections/nspire-health-ltd/55184c08-432f-4ed6-a6e8-b954ea332580)

Company: https://www.keypedia.com/companies/nspire-health-ltd/ca039fa9-8db5-463b-a56c-f278c4920e95

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7